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A note on interpretation. VAERS reports are unverified and may be incomplete or coincidental. A report does not establish that a vaccine caused an event, and counts should not be used to calculate incidence or infer causation. Full disclaimer

1,929,324 reports(835 ms)

#2829489Mar 4, 2025
Female·Age unknown·CA·TYP

The patient felt completely down for the day after taking Vivotif; The patient was not able to continue with Vivotif administration; Stomach cramps and pain in the belly; Diarrhea (ten to 15 times); Vomiting (ten to 15 times); Headache; Fatigue, Completely dra…

Abdominal pain upperDiarrhoeaFatigueHeadacheIncomplete course of vaccinationVomiting
#2829490Mar 4, 2025
Female·Age unknown·NH·TYP

The patient only took three out of four doses of Vivotif before the medication was lost; Case reference number US-BN-2024-000644 is a spontaneous case report initially received from a pharmacist via Med Communications (reference number: USBAV24-0532) on 18-Mar…

Product dose omission issue
#2829491Mar 4, 2025
Male·Age unknown·CA·TYP

The reporter took first dose of Vivotif which was three days in the counter, maximum temperature reached 70 Fahrenheit; The reporter took first dose of Vivotif which was three days in the counter, maximum temperature reached 70 Fahrenheit; Case reference numbe…

Incorrect dose administered
#2829492Mar 4, 2025
Female·Age unknown·WA·TYP

The patient took first and the second dose of Vivotif which was left at room temperature at 65 Fahrenheit about four of five days; The patient took first and the second dose of Vivotif which was left at room temperature at 65 Fahrenheit about four of five days…

Inappropriate schedule of product administrationNo adverse eventProduct storage error
#2829493Mar 4, 2025
Female·Age unknown·MN·TYP

Patient took first two capsules on two consecutive days; Case reference number US-BN-2024-000675 is a spontaneous case report initially received from a pharmacist via Med Communication (reference number: USBAV24-0560) on 25-Mar-2024 and concerns a female patie…

Inappropriate schedule of product administrationNo adverse event
#2829494Mar 4, 2025
Female·Age unknown·MN·TYP

The patient took one dose of Vivotif vaccine which was left at ambient temperature for six hours, maximum temperature was 68 Fahrenheit; The patient took one dose of Vivotif vaccine which was left at ambient temperature for six hours, maximum temperature was 6…

Product storage error
#2829495Mar 4, 2025
Unknown·Age unknown·UT·TYP

Four patients did not take the fourth dose of Vivotif as the box of pills was lost; Case reference number US-BN-2024-001737 is a spontaneous case report initially received from a nurse via Med Communication (reference number: USBAV24-0596) on 29-Mar-2024 and c…

Incomplete course of vaccination
#2829496Mar 4, 2025
Male·Age unknown·TN·TYP

Patient could not tolerate the Vivotif, vomited and was nauseated all day; Patient could not tolerate the Vivotif, vomited and was nauseated all day; Patient could not tolerate the Vivotif, vomited and was nauseated all day; Case reference number US-BN-2024-00…

Drug intoleranceNauseaVomiting
#2829497Mar 4, 2025
Female·Age unknown·OR·TYP

The patient took the second dose of Vivotif one day after the first dose; Case reference number US-BN-2024-001741 is a spontaneous case report initially received from a consumer via Med Communications (reference number USBAV24-0608) on 01-Apr-2024 and concerns…

No adverse eventProduct administered to patient of inappropriate age
#2829498Mar 4, 2025
Female·Age unknown·CA·TYP

The patient left Vivotif vaccine at room temperature for four days, maximum temperature was 65 Fahrenheit; The patient left Vivotif vaccine at room temperature for four days, maximum temperature was 65 Fahrenheit; Case reference number US-BN-2024-001746 is a s…

Product storage error
#2829499Mar 4, 2025
Unknown·Age unknown·OR·TYP

The patient took dose of Vivotif vaccine one consecutive days; Case reference number US-BN-2024-001747 is a spontaneous case report initially received from a pharmacist via Med Communications (reference number USBAV24-0615) on 01-Apr-2024 and concerns a patien…

Product administered to patient of inappropriate age
#2829500Mar 4, 2025
Male·Age unknown·UT·TYP

The patient took first and second dose of Vivotif and went out of town for four days and wanted to know if the vaccination can be resumed; Case reference number US-BN-2024-001748 is a spontaneous case report initially received from a nurse via Med Communicatio…

Inappropriate schedule of product administration
#2829501Mar 4, 2025
Male·Age unknown·GA·TYP

The patient took two doses of Vivotif vaccine which left at room temperature for over 72 hours, maximum temperature reached was room temperature 70 Fahrenheit; The patient took two doses of Vivotif vaccine which left at room temperature for over 72 hours, maxi…

Product storage error
#2829502Mar 4, 2025
Female·Age unknown·MA·TYP

The patient had diarrhea after first two doses of Vivotif vaccine; The patient received three doses of Vivotif vaccine and did not want to take the fourth dose; Case reference number US-BN-2024-001760 is a spontaneous case report initially received from other…

DiarrhoeaIncomplete course of vaccination
#2829503Mar 4, 2025
Male·Age unknown·TN·TYP

The patient took two capsules of Vivotif which were left at room temperature for almost three weeks; The patient took two capsules of Vivotif which were left at room temperature for almost three weeks; Case reference number US-BN-2024-001762 is a spontaneous c…

Product storage error
#2829504Mar 4, 2025
Male·Age unknown·CO·TYP

The patient experienced some abdominal pain with cramping; Case reference number US-BN-2024-001773 is a spontaneous case report initially received from other health care professional via Med Communications (reference number USBAV24-0671) on 05-Apr-2024 and con…

Abdominal pain
#2829505Mar 4, 2025
Male·Age unknown·WA·TYP

The patient ate five minutes after took Vivotif; Case reference number US-BN-2024-001774 is a spontaneous case report initially received from a pharmacist via Med Communications (reference number USBAV24-0686) on 08-Apr-2024 and concerns a 53-years-old male pa…

Product administration error
#2829506Mar 4, 2025
Male·Age unknown·CA·TYP

The patient was unable to take the scheduled fourth dose of Vivotif; The patient received Vivotif and killed Typhoid vaccine; The patient felt mildly unwell after first dose of Vivotif; The patient become extremely nauseous and vomited after second dose of Viv…

Incomplete course of vaccinationInterchange of vaccine productsMalaiseNauseaVomiting
#2829507Mar 4, 2025
Female·Age unknown·CA·TYP

Vivotif vaccine was stored at approximately 70 Fahrenheit degrees for at least 24 hours and the patient already started treatment; Vivotif vaccine was stored at approximately 70 Fahrenheit degrees for at least 24 hours and the patient already started treatment…

Product storage error
#2829508Mar 4, 2025
Male·Age unknown·NC·TYP

Patient had tested positive to COVID and had some mild congestion, cough and no other symptoms; Case reference number US-BN-2024-001786 is a spontaneous case report initially received from a nurse via Med Communication (reference number: USBAV24-0707) on 10-Ap…

COVID-19CoughPyrexiaRespiratory tract congestionSARS-CoV-2 test positive
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